Mutated penicillin expandase and process for preparing 7-ADCA using the same

ABSTRACT

A mutated expandase enzyme having higher activity on penicillin G is provided to produce phenylacetyl-7-aminodeacetoxycephalosporanic acid (7-ADCA), which mutated expandase enzyme has one or more amino acid substitutions selected form M73T, S79E, V275I, L277K, C281Y, G300V, N304K, I305L and I305M.

FIELD OF THE INVENTION

[0001] The present invention relates to a mutated penicillin expandase having high substrate specificity to penicillin G, recombinant cells expressing the mutated expandase, and a process of preparing 7-aminodeacetoxycephalosporanic acid (7-ADCA) using the mutated expandase.

BACKGROUND OF THE INVENTION

[0002] 7-aminodeacetoxycephalosporanic acid (7-ADCA) is one of the important intermediates for the production of cephalosporins cefalexin, cefradine, and cefadroxil which are antibiotic compounds commonly and long used in humans and animals. The industrial process to synthesize 7-ADCA mainly includes two steps: a chemical ring expansion of penicillin G to phenylacetyl-7-ADCA and an enzymatic side chain cleavage of phenylacetyl-7-ADCA. However, the chemical reaction of the ring expansion is complex and expensive, and the by-products and the organic solvents (such as pyridine and HBr) are toxic to the environment. Therefore, an enzymatic reaction is greatly desirable to replace such chemical reaction.

[0003] It has been reported that a natural enzyme, deacetoxycephalosporain C synthase (DAOCS, or expandase), may be responsible for the catalysis of the expansion reaction. Streptomyces sp. (such as Streptomyces clavuligerus, Streptomyces ambofaciens and Streptomyces chartreusis) can produce the expandase. As illustrated in EP-A-0341892, the expandase can be obtained from Streptomyces clavuligerus, and has been cloned. The expandase has been well studied for its chemical and functional properties, see EP-A-0366354. Unfortunately, the native expandase has less substrate specificity to penicillin G than the normal substrate penicillin N (Rollins, M. J. et al., Can. J. Microbiol. 34: 1196-1202 (1988) and Crawford, L., et al., Bio/Technology, 13: 58-62 (1995)). Penicillin G is commercially available at a low cost. In contrast, penicillin N is expensive and not easily available. Furthermore, even though penicillin N is expanded, its side chain cannot be easily removed. Accordingly, the chemical synthesis of 7-ADCA, rather than an enzymatical synthesis, is still used in industrial production.

[0004] There are a number of applications directed to producing 7-ADCA by expandase. U.S. Pat. No. 5,731,165 describes a process for the preparation and recovery of 7-ADCA via enzymatic ring expansion activity on penicillin G, using a Penicillium chrysogenum transformant strain expressing expandase. U.S. Pat. No. 5,559,005 discloses a bioprocess for preparing 7-amino-cephalosporanic acid (7-ACA) or 7-ADCA using a transformed stain of Penicillium chrysogenum having expandase activity capable of accepting adipoyl-6-amino-penicillanic acid (adipoyl-6-APA) as a substrate. Nevertheless, since both adipoyl-6-APA and penicillin G are poor substrates for native expandase in vitro (U.S. Pat. No. 5,559,005), it is not optimistic to have a high expansion efficiency while applied in vivo.

[0005] Recently, Chih H. S. et al. (Biochemical and Biophysical Research Communications, 287: 507-513 (2001)) discloses a mutated DAOCS comprising an amino acid substitution of N304L. U.S. Pat. No. 5,919,680 describes a mutated expandase which has an altered amino acid sequence from a native expandase, resulting in an altered substrate specificity. Several amino acid positions have been mentioned in that patent, and the mutated expandase created by changing one or more of the mentioned amino acids shows a higher activity ratio of penicillin G to penicillin N in a mixture of these two substrates, but has a lower activity on penicillin G and penicillin N individually than wild-type expandase. Therefore, there is still a need to develop a mutated penicillin expandase having more substrate specificity and enzymatic activity on penicillin G.

SUMMARY OF THE INVENTION

[0006] The present invention provides mutated expandase having expansion activities 2 to 32 folds higher on penicillin G than wild-type expandase.

[0007] One object of the invention is to provide a mutated penicillin expandase which comprises an amino acid substitution at one or more residue positions corresponding to those of a wild-type expandase selected is from the group consisting of methionine 73, serine 79, valine 275, leucine 277, cysteine 281, glycine 300, asparagine 304 and isoleucine 305, provided that the amino acid substitution at the residue position of asparagine 304 is not N304L. In particular, the invention provides a mutated penicillin expandase which comprises one or more specific amino acid substitutions selected from the group consisting of M73T, S79E, V275I, L277K, C281Y, G300V, N304K, I305L and I305M, wherein the residue positions of the amino acid substitution correspond to those of a wild-type expandase.

[0008] Another object of the invention is to provide an isolated nucleic acid molecule encoding the mutated penicillin expandase.

[0009] Another object of the invention is to provide a recombinant vector comprising the nucleic acid molecule of the invention and a regulatory sequence operatively linked thereto.

[0010] Still another object of the invention is to provide recombinant cells comprising the nucleic acid molecule of the invention.

[0011] In another aspect, the invention provides a method to produce a mutated penicillin expandase. In one embodiment of the invention, the method comprises expressing the nucleic acid molecule of the invention and recovering the mutated penicillin expandase. In another embodiment of the invention, the method comprises culturing the recombinant cells of the invention to express the mutated penicillin expandase and recovering the mutated penicillin expandase form the cell culture.

[0012] In another aspect, the invention provides a process for producing 7-ADCA comprising treating penicillin G with the mutated penicillin expandase of the invention to produce phenylacetyl-7-ADCA, followed by deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA.

[0013] In still another aspect, the invention provides a process for producing 7-ADCA, which process comprises the steps of (a) cultivating penicillin G producing cells which is transformed with the nucleic acid molecule of the invention under conditions suitable for production of penicillin G and expression of the mutated penicillin expandase such that the penicillin G is expanded by the mutated expandase and phenylacetyl-7-ADCA is produced; (b) deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA.

[0014] The present invention will be fully understood from the detailed description and figures as given below.

BRIEF DESCRIPTION OF THE DRAWINGS

[0015]FIG. 1 shows the SDS-PAGE results of the purified DAOCS of the invention. Lanes 1 to 9 represent molecular weight markers and the purified DAOCS of YS5, YS8, YS11, YS12, YS16, YS49, YS53 and YS59 mutants, respectively. Each loaded DAOCS dose was in an amount of 5 μg.

[0016]FIG. 2 shows the SDS-PAGE results of the purified DAOCS of the invention. Lanes 1 and 2 represent molecular weight markers and the purified DAOCS of YS67 mutant, respectively. The loaded DAOCS dose was in an amount of 5 μg.

[0017]FIG. 3 shows the SDS-PAGE results of the purified DAOCS of the invention. Lanes 1 represents molecular weight markers. Lanes 2 to 5 represent samples irrelevant to the invention. Lanes 6 and 7 represent the purified DAOCS of SC29 and SC39 mutants, respectively. The loaded DAOCS dose was in an amount of 5 μg.

[0018]FIG. 4 shows the SDS-PAGE results of the purified DAOCS of the invention. Lanes 1 represents molecular weight markers. Lanes 2 to 5 represent samples irrelevant to the invention. Lanes 6 to 9 represent the purified DAOCS of YS 98, YS108, YS115 and YS125, respectively. The loaded DAOCS dose was in an amount of 5 μg.

DETAILED DESCRIPTION OF THE INVENTION

[0019] The primary aspect of the present is to provide a mutated penicillin expandase having a better substrate specificity to penicillin G, wherein the mutated penicillin expandase comprises an amino acid substitution at one or more residual positions corresponding to those in a wild-type expandase selected from the group consisting of methionine 73, serine 79, valine 275, leucine 277, cysteine 281, glycine 300, asparagine 304 and isoleucine 305, provided that the amino acid substitution at the residue position of asparagine 304 is not N304L. More specifically, the invention provides a mutated penicillin expandase comprising one or more amino acid substitutions selected from the group consisting of M73T, S79E, V275I, L277K, C281Y, G300V, N304K, I305L and I305M.

[0020] A “wild type penicillin expandase”, as used herein, refers to the native penicillin expandase obtained from Streptomyces sp. Preferably, the wild-type expandase is obtained from Streptomyces clavuligerus. The native penicillin expandase and its corresponding gene (cefE gene) have been well characterized and described in the prior art (e.g., EP-A-0366354 and EP-A-0341892). Persons skilled in the art can readily obtain the nucleic acid sequences of the wild-type penicillin expandase and the corresponding amino acid sequences from the prior art.

[0021] The mutated penicillin expandase of the invention comprises the functional equivalents of the same. As used herein, the “functional equivalents” of the mutated penicillin expandase may contain further amino acid mutations (e.g., deletions, additions or substitutions) located at positions other than those described above, wherein said further amino acid mutations result in silent changes and thus do not substantially affect the function (e.g., enzyme activity) of the mutated penicillin expandase. Furthermore, in the “functional equivalents” of the mutated penicillin expandase, the specific amino acid substitutions (i.e., selected from M73T, S79E, V275I, L277K, C281Y, G300V, N304K, I305L and I305M) may be exchanged with other amino acid substitutions of similar characteristics which result in a silent change. For example, a mutated penicillin expandase with an amino acid substitution of “S79D” is functional equivalent to that with an amino acid substitution of “S79E,” since the amino acid D (aspartic acid) and E (glutamic acid) are both classified as acid amino acids and are of similar characteristics.

[0022] In another aspect, the invention provides an isolated nucleic acid molecule encoding the mutated penicillin expandase of the invention. The isolated nucleic acid molecule of the invention is obtained by mutating the nucleic acid encoding the wild-type penicillin expandase. A conventional mutation-inducing technical is well known in the art, such as irradiation of with gamma rays or ultraviolet light or treatment with a mutagen, such as hydroxylamine and ethylmethane, or site-directed mutagenesis. Persons skilled in the art can choose a suitable mutagenesis technology to obtain a mutated nucleic acid molecule. The mutated nucleic acid molecules can be further cloned and selected for their biological activities. More detailed technologies, comprising mutagenesis, cloning and screening for biological activities, used to obtain the isolated nucleic acid molecules of the invention are described in the following examples.

[0023] According to the invention, the isolated nucleic acid may be inserted into a vector to form a recombinant vector. The term “vector” used herein means a nucleic acid molecule, which is capable of carrying and transferring a nucleic acid segment of interest into a host cell for the purpose of expression or replication of the same. In particular, a vector refers to a plasmid, cosmid, bacteriophage or virus. Typically, the nucleic acid segment of interest is operatively linked to a regulatory sequence such that, when introducing into a host cell, for instance, the nucleic acid segment can be expressed in the host cell under the control of the regulatory sequence. The regulatory sequence may comprise, for example, to a promoter sequence (e.g., cytomegalovirus (CNV) promoter, simian virus 40 (SV40) early promoter and T7 promoter), replication origin and other control sequences (e.g., Shine-Dalgano sequences and termination sequences). Preferably, the nucleic acid segment of interest may be connected to another nucleic acid fragment such that a fused polypeptide is (e.g., His-tag fused polypeptide) is produced and beneficial to the subsequent purification procedures. The method for identifying and selecting the regulatory sequences are well known to the skilled persons and widely described in the literatures. The skilled persons can readily construct the recombinant vector of the invention according to the specification and the well-known technologies.

[0024] The recombinant vector of the invention can be introduced into host cells to produce the mutated penicillin expandase. Accordingly, recombinant cells transformed with the recombinant vector is within the scope of the invention. Such recombinant cells can be prokaryotic (e.g., bacteria) or eukaryotic (e.g., fungi, animal and plant cells). In particular, the recombinant cells of the invention are penicillin G producing cells, preferably Penicillium chrysogenum cells, which can be used to produce 7-ADCA in vivo, as described below. A number of transformation technologies, such as a calcium chloride treatment, Calcium-PEG procedure, electroporation, DEAE-dextrin-mediated transfection, lipofection and microinjection are well described in many literatures. The skilled persons can choose a proper technology depending on the nature of the host cells and the vector to be introduced in the host cells.

[0025] A method for producing the mutated penicillin expandase is also provided in the invention. The recombinant cells described above can be cultured in a suitable condition to express the mutated penicillin expandase and then the expressed expandase is recovered and purified. Those skilled in this art will appreciate that the recovering and purifying method is widely described in many references and is not limited, for example, by various chromatographies (e.g., HPLC or affinity columns).

[0026] The genetic engineering methods mentioned above such as DNA mutagenesis, cloning, vector construction, transformation, protein expression, and purification can be accomplished by those skilled in this art, and which can be seen, for example, in Molecular Cloning: A Laboratory Manual, 2d ed., Cold Spring Harbor Laboratory Press, Sambrook, J., E. F. Fritsch and T. Maniatis eds. (1989).

[0027] The present invention is also related to a process to produce 7-ADCA, which process comprises the steps of treating penicillin G with the mutated penicillin expandase of the invention to produce phenylacetyl-7-ADCA and deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA. In particular, the mutated expandase is expressed and recovered as stated above, and then added with the substrate penicillin G. The mixture is incubated under conditions (e.g., at a temperature of 30° C.) suitable for the enzyme activity of the mutated expandase such that a ring expansion reaction is conducted by the mutated expandase and the substrate penicillin G is converted to phenylacetyl-7-ADCA. Preferably, phenylacetyl-7-ADCA is purified through a simple solvent extraction, for example, and then treated with a suitable enzyme (e.g., penicillin amidase, as described in EP-A-0453047) such that the phenylacetyl side chain is removed and the desired 7-ADCA is obtained. In another aspect, the to substrate penicillin G can be directly added into the cell culture of the recombinant cells expressing the mutated expandase of the invention. The expressed expandase then reacts with the penicillin G and converts it into phenylacetyl-7-ADCA, followed by deacylation of the phenylacetyl-7-ADCA to produce the desired 7-ADCA. It has been found that penicillin G producing cells (e.g., Penicillium chzysogenum) transformed with an expandase-encoding gene is capable of producing phenylacetyl-7-ADCA in vivo. Accordingly, another aspect of the invention is to provide a process to produce 7-ADCA using penicillin G producing cells, which process comprises the steps of (a) cultivating penicillin G producing cells which is transformed with the recombinant vector of the invention under conditions suitable for production of penicillin G and expression of the mutated expandase of the invention such that the penicillin G is expanded by the mutated expandase and phenylacetyl-7-ADCA is produced; (b) deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA. The term “penicillin G producing cells” used herein refers to cells capable of naturally producing penicillin G in a normal condition without any genetic engineering technologies (e.g., transformation). Preferably, the penicillin G producing cells are cells of Penicillium chrysogenum. The phenylacetyl-7-ADCA produced from Step (a) can be optionally purified by filtration and extraction steps. The detailed procedures, such as transformation and fermentation of such cells and purification of the produced phenylacetyl-7-ADCA, have been described in the prior art, such as U.S. Pat. No. 5,919,680 and EP 5,731,165 which are incorporated herein for reference.

EXAMPLES

[0028] The present invention will become apparent with reference to the examples below. The examples described below are given by way of illustration only and are not intended to be any limitation of the present invention.

[0029] Materials

[0030] All chemicals were purchased from Merck unless stated otherwise. Strain Streptomyces clavuligerus was ordered from Culture Collection & Research Center (Taiwan). Oligonucleotides were synthesized by Genset (Singapore Biotech). DNA sequences were analyzed by Mission Biotech (Taiwan). Liquid chromatography—Mass analysis was performed by Protech Laboratory (Taiwan). Penicillin G was from Harbin Pharmaceutical Co. (China). C¹⁴-penicillin G was ordered from Moravek. Penicillin N, deacetoxycephalosporin C, and cephalosporin G were synthesized in this laboratory. Other materials and supplied companies are indicated as follow: enzymes for DNA manipulation (Promega); Zero Blunt TOPO PCR cloning kit (Invitrogen); DNA gel extraction kit, GFX -Micro Plasmid Prep kit, & FPLC apparatus and columns (Amersham Pharmacia Biotech Inc.); PCR clean up-M (Viogene); pET24a, pET30a, BL21(DE3), and Tuner cells (Novagen); Bradford reagent, 30% acrylamide/bis-acrylamide solution, and PAGE apparatus (Bio-Rad); HPLC set (LC-10AT, Sil-10AD, SPD-10A; Shimadzu); C₁₈ column (250×4.6 mm, 5μ; Hypersil); HPLC data analysis software (Scientific Information Service Corporation); pefabloc SC, and leupeptin (Roche)

Example 1 Random Mutagenesis

[0031] The cefE gene fragment was cut off from pYB4, a pET24a backbone with a BamHI-Hind III cefE insert cloned from Streptomyces clavuligerus using Zero Blunt TOPO PCR Cloning kit, treated with 0.8 M hydroxylamine at 65° C. for 2 hours, cleaned up with PCR Clean up-M kit, then ligated back into the backbone vector. This mutated cefE pool was transformed into BL21(DE3) by electroporation, and transformants were selected on LB plates with 50 μg/ml of kanamycin. The mutated transformants were subjected for an activity improvement screening.

Example 2 Activity Improvement Screening

[0032] The mutated transformants were grown in a 96-well plate containing 56.7 μl of LB medium with kanamycin in each well. Then 0.1 mM IPTG was added into each well to induce DAOCS indirectly at 30° C. for 2 hours of shaking, followed by another 1 hour of shaking after an addition of 7 μl of 100 mg/ml lysozyme. The activity of DAOCS was measured by an addition of 30 μl of assay mixture (500 mM Mops/pH 7.0, 18 mM FeSO₄, 40 mM ascorbate, 25.6 mM α-ketoglutarate and suitable amount of penicillin G), and incubated at 30° C. for another 1 hour of shaking. The resulting mixture was loaded on an 8 mm thick paper disc, and placed onto a bioassay plate seeded with Escherichia coli ESS strain (a β-lactam supersensitive mutant, a gift from Dr. Demain) as described in Cho H. et al., Proc. Natl. Acad. Sci. USA, 95: 11544-11548 (1988). The transformants with clear zone bigger than that of unmutated control strain were selected and subjected for further activity confirmation by TLC. After the activity improvement screening, the mutated cefE was manipulated into a NdeI-Hind III insertion version in the same vector (pET24a), and the mutants such as YS5 (V275I), YS53 (C281Y) and YS59 (S79E) were selected.

[0033] A TLC method to separate penicillin G and cephalosporin G was also developed for bioassay screening. Silica plates 60 F254 were used as a solid phase and the mobile phase was a mixture of chloroform: acetone: acetic acid=6:5:0.5 (volume ratio). C¹⁴ labeled penicillin G was used in the standard assay with 20 μg of cell extract (quantitated with Bio-Rad Bradford kit using BSA as a standard), and after addition of ethanol the mixture was applied directly onto TLC plate without centrifugation.

Example 3 Site-Directed Mutagenesis

[0034] The wild-type expandase gene (i.e., ceJE) was PCR cloned from Streptomyces clavuligerus and inserted into pET30a Ndel-Hind III site, and the resulted plasmid was designated as pYS16. The Quick Change Mutagenesis Kit was used to produce site-directed mutants of pYS16. The mutated sites were chosen based on the crystal structure of DAOCS (Valegard K. et al., Nature, 394: 805-809 (1998)) using Swiss-Pdb Viewer (V3.7b2) program by selecting residuals surrounding active center within 10 Å. Each site was changed to Ala residual first, then a positive charge residual, a hydrophobic residual and a sulfur-containing residual. The primers were designed according to the manufacturer's manual. The resulted mutants were confirmed by DNA sequencing the harbored plasmids, and the cell crude extracts were prepared and subjected for DAOCS activity assay.

Example 4 DAOCS Activity Assays

[0035] BL21(DE3) transformants were grown overnight in 5 ml of LB medium with 50 μg/ml kanamycin at 30° C. This culture was used to inoculate 100 ml of the same medium and grown at 30° C. for 1 hour. Then 0.1 mM IPTG was added to induce DAOCS indirectly at 30° C. for 4 hours. Cells were harvested, washed with buffer A (50 mM Mops/pH 7.5, 1 mM PMSF, 1 mM DTT, and 0.5 μg/ml leupeptin), lysed by sonication (VCX 750; Sonics & Materials, USA), and centrifuged at 15,000× g for 15 minutes. The supernatant was used as a cell extract.

[0036] For penicillin G, 20 μl of cell extracts was added into a standard 200 μl assay reaction containing 50 mM Mops/pH 7.5, 4 mM ascorbate, 1 mM FeSO₄, 4 mM α-ketoglutarate and 7 mM penicillin G, and incubated at 30° C. for 20 minutes. The reaction was stopped by addition of 200 μl of ethanol, followed by a centrifugation at 15,000× g for 5 minutes. The concentration of cephalosporin G in supernatant was analyzed by HPLC with 40 μl injection. The mobile phase was 25 mM potassium phosphate/pH 6.5 with 19% acetonitrile at a flow rate of 1 ml/min. The retention time for cephalosporin G was 8.5 minutes and 12.5 minutes for penicillin G with detection at 215 nm, and the product at 8.5 minutes in DAOCS reaction was confirmed by LC-MS to have a molecular weight of 370. The site-directed mutants such as YS49 (L277K), YS8 (I305L), YS11 (I305M), and Y12 (N304K) having higher expandase activities on penicillin G than the parent strain YS16 were obtained. The different combinations of the mutated amino acids mentioned above were also constructed by site-directed mutagenesis.

Example 5 DAOCS Purification

[0037] The cell extract (2 ml) of a candidate mutant was applied onto a HiTrap Q column (5 ml) equilibrated with buffer B (50 mM Mops/pH 7.5, 1 mM DTT, 0.4 mM pefabloc SC, and 0.5 μg/ml leupeptin). Then, the column was washed with 20 ml of buffer B, followed by a further wash with 25 ml of 120 mM NaCl in buffer B, and DAOCS was eluted off with 20 ml of 150 mM NaCl in buffer B. The DAOCS containing fractions were pooled (10 ml), concentrated by UF 15 device (NMWL 5K; Millipore), and loaded onto a Hiload Superdex 75 (1-6/60) column pre-equilibrated with buffer B at a flow rate at 1 ml/min. The DAOCS thus purified had a purity more than 90% as judged by SDS-PAGE, see FIGS. 1 and 2, and was stored in 1 mM DTT and 2 mg/ml BSA at −80° C. immediately.

Example 6 Kinetic Assays of Purified DAOCS

[0038] The standard penicillin G assay was followed for Kinetic assay, but 20 μg of purified DAOCS was used and the concentration of α-ketoglutarate was reduced to 1 mM. Kinetic parameters were obtained from triplicate experiments by Hanes-Woolf Plot. For assays using penicillin N as main substrate, a total volume of 240 μl reaction containing 50 mM Hepes/pH 7.5, 0.4 mM ascorbate, 0.1 mM FeSO₄, 0.1 mM α-ketoglutarate, 0.1 mM penicillin N and 05 μg of purified DAOCS was incubated at 30° C. for 10 minutes, then the same volume of 10 mM EDTA/pH 7.5 was added, and the mixture was subjected to ultrafiltration with UF 0.5 device (NMWL 5000, Millipore). The filtrate was analyzed by HPLC using 25 mM potassium phosphate/pH 6.5 as a mobile phase. The retention time of DAOC and penicillin N was 12 minutes and 13.5 minutes, respectively. The results of kinetic parameters are shown in Table 1, wherein the definition and calculation of the parameters are described in Lehninger et al. Principles of Biochemistry, 2.sup.nd Ed. Worth Publishers, New York (1993) which is incorporated herein for reference. TABLE 1 Kinetic parameters for penicillin N and penicillin G Strains Km (mM) k_(cat)(S⁻¹) k_(cat)/Km (M⁻¹S⁻¹) For penicillin N: YS16 (wild-type) 0.014 ± 0.006 0.307 ± 0.038 22,000 YS5(V275I) 0.012 ± 0.003 0.252 ± 0.020 20,000 YS8(I305L) 0.006 ± 0.002 0.284 ± 0.030 44,000 YS11(I305M) 0.012 ± 0.001 0.310 ± 0.004 26,000 YS12 (N304K) 0.004 ± 0.001 0.366 ± 0.023 92,000 YS125(N304L) 0.018 ± 0.004 0.415 ± 0.063 23,000 YS49(L277K) 0.011 ± 0.005 0.220 ± 0.042 20,000 YS53(C281Y) 0.006 ± 0.001 0.273 ± 0.014 47,000 YS59(S79E) 0.009 ± 0.003 0.178 ± 0.019 20,000 YS115(M73T) 0.006 ± 0.003 0.239 ± 0.009 40,000 YS67 0.013 ± 0.005 0.316 ± 0.032 24,000 (V275I & I305M) For penicillin G: YS16 (wild-type) 2.58 ± 0.22 0.0302 ± 0.0007 12 YS5(V275I) 1.68 ± 0.20 0.0335 ± 0.0008 20 YS8(I305L) 0.66 ± 0.07 0.0506 ± 0.0010 77 YS11(I305M) 0.75 ± 0.04 0.0968 ± 0.0013 129 YS12 (N304K) 0.22 ± 0.03 0.0376 ± 0.0002 171 YS125(N304L) 0.55 ± 0.12 0.0268 ± 0.0004 49 YS49(L277K) 0.72 ± 0.02 0.0343 ± 0.0005 48 YS53(C281Y) 0.68 ± 0.34 0.0496 ± 0.0022 73 YS59(S79E) 0.75 ± 0.02 0.0210 ± 0.0002 28 YS115(M73T) 0.74 ± 0.16 0.0418 ± 0.0014 56 YS67 0.25 ± 0.08 0.0972 ± 0.025  389 (V275I & I305M)

[0039] As shown in Table 1, all mutants have expansion activities 2 to 32 folds higher on penicillin G than wild-type expandase as implicated in k_(cat)/Km (M⁻¹S⁻¹) parameters. In contrast, these mutants do not cause significant changes in kinetic parameters obtained with penicillin N, except for mutant YS12 which has expansion activities 4 folds higher than wild-type YS16. Making a comparison between YS12 (N304K) of the invention and YS125 (N304L) as disclosed in Chih H. S. et al sitpra, YS125 has the expansion activity 4 folds higher on penicillin G than wild-type expandase, and YS12 has the expansion activity 14 folds higher on penicillin G than wild-type expandase.

[0040] The relative activities of the mutants are determined according to Chih H. S. et al supra with the activity of wild-type DAOCS as 100% and shown in Table 2. The assay was performed with 1 mM penicillin G, and the other conditions were the same as standard assay. TABLE 2 The relative activities of purified combinated mutants compared to wild type DAOCS Strains Mutated sites Relative Activities (%) YS16 — 100 YS67 275I, 305M 500 YS74 275I, 304K, 305L 300 YS81 275I, 281Y, 305M 1290 YS88 79E, 275I, 281Y 430 YS94 281Y, 304K, 305M 650 YS96 79E, 275I, 305M 1110 YS100 79E, 275I, 305L 470 YS76 79E, 275I, 281Y, 305L 250 YS108 300V 410 SC29 275I, 281Y, 300V 620 SC39 73T, 281Y 610

[0041]

1 1 1 1230 DNA Streptomyces clavuligerus CDS (232)...(1164) 1 cccgggtgcc gctggtcagc gccaccggat cgacccgtat gggccgcgcc gtgggccccc 60 gggccggtgc tccggatctc ggcgaacttc tacaccaccg aagaggagat cgaccgcctg 120 gcggacgcgc tggacgcgct gacgggcgag tgatcccccc ggctcgcgga ccgcctcccc 180 cgcgctgttg accacccggt tcacggatta cgagaggatc agtgagagtt g atg gac 237 Met Asp 1 acg acg gtg ccc acc ttc agc ctg gcc gaa ctc cag cag ggc ctg cac 285 Thr Thr Val Pro Thr Phe Ser Leu Ala Glu Leu Gln Gln Gly Leu His 5 10 15 cag gac gag ttc cgc agg tgt ctg agg gac aag ggc ctc ttc tat ctg 333 Gln Asp Glu Phe Arg Arg Cys Leu Arg Asp Lys Gly Leu Phe Tyr Leu 20 25 30 acg gac tgc ggt ctg acc gac acc gag ctg aag tcg gcc aag gac atc 381 Thr Asp Cys Gly Leu Thr Asp Thr Glu Leu Lys Ser Ala Lys Asp Ile 35 40 45 50 gtc atc gac ttc ttc gag cac ggc agc gag gcg gag aag cgc gcc gtc 429 Val Ile Asp Phe Phe Glu His Gly Ser Glu Ala Glu Lys Arg Ala Val 55 60 65 acc tcg ccc gtc ccc acc atg cgc cgc ggc ttc acc ggg ctg gag tcg 477 Thr Ser Pro Val Pro Thr Met Arg Arg Gly Phe Thr Gly Leu Glu Ser 70 75 80 gag agc acc gcc cag atc acc aat acc ggc agc tac tcc gac tac tcg 525 Glu Ser Thr Ala Gln Ile Thr Asn Thr Gly Ser Tyr Ser Asp Tyr Ser 85 90 95 atg tgc tac tcg atg ggc acc gcg gac aac ctc ttc ccg tcc ggt gac 573 Met Cys Tyr Ser Met Gly Thr Ala Asp Asn Leu Phe Pro Ser Gly Asp 100 105 110 ttc gag cgg atc tgg acc cag tac ttc gac cgc cag tac acc gcc tcc 621 Phe Glu Arg Ile Trp Thr Gln Tyr Phe Asp Arg Gln Tyr Thr Ala Ser 115 120 125 130 cgc gcg gtc gcc cgg gag gtc ctg cgg gcg acc ggg acc gag ccc gac 669 Arg Ala Val Ala Arg Glu Val Leu Arg Ala Thr Gly Thr Glu Pro Asp 135 140 145 ggc ggg gtc gag gcc ttc ctc gac tgc gag ccg ctg ctg cgg ttc cgc 717 Gly Gly Val Glu Ala Phe Leu Asp Cys Glu Pro Leu Leu Arg Phe Arg 150 155 160 tac ttc ccg cag gtc ccc gag cac cgc agc gcc gag gag cag ccc ctg 765 Tyr Phe Pro Gln Val Pro Glu His Arg Ser Ala Glu Glu Gln Pro Leu 165 170 175 cgg atg gcg ccg cac tac gac ctg tcg atg gtc acc ctc atc cag cag 813 Arg Met Ala Pro His Tyr Asp Leu Ser Met Val Thr Leu Ile Gln Gln 180 185 190 aca ccc tgc gcc aac ggc ttc gtc agc ctc cag gcc gag gtc ggc ggc 861 Thr Pro Cys Ala Asn Gly Phe Val Ser Leu Gln Ala Glu Val Gly Gly 195 200 205 210 gcg ttc acg gac ctg ccc tac cgt ccg gac gcc gtc ctc gtc ttc tgc 909 Ala Phe Thr Asp Leu Pro Tyr Arg Pro Asp Ala Val Leu Val Phe Cys 215 220 225 ggc gcc atc gcg acc ctg gtg acc ggc ggc cag gtc aag gcc ccc cgg 957 Gly Ala Ile Ala Thr Leu Val Thr Gly Gly Gln Val Lys Ala Pro Arg 230 235 240 cac cat gtc gcg gcc ccc cgc agg gac cag ata gcg ggc agc agc cgc 1005 His His Val Ala Ala Pro Arg Arg Asp Gln Ile Ala Gly Ser Ser Arg 245 250 255 acc tcc agt gtg ttc ttc ctc cgt ccc aac gcg gac ttc acc ttc tcc 1053 Thr Ser Ser Val Phe Phe Leu Arg Pro Asn Ala Asp Phe Thr Phe Ser 260 265 270 gtc ccg ctg gcg cgc gag tgc ggc ttc gat gtc agc ctg gac ggc gag 1101 Val Pro Leu Ala Arg Glu Cys Gly Phe Asp Val Ser Leu Asp Gly Glu 275 280 285 290 acc gcc acg ttc cag gat tgg atc ggg ggc aac tac gtg aac atc cgc 1149 Thr Ala Thr Phe Gln Asp Trp Ile Gly Gly Asn Tyr Val Asn Ile Arg 295 300 305 cgc aca tcc aag gca tagagagcac acaccgtcat ggtcacagca gcaatcagtg 1204 Arg Thr Ser Lys Ala 310 gtaccgacga gatacgcgcg agggcg 1230 

What is claimed is:
 1. A mutated penicillin expandase comprising an amino acid substitution at one or more residue positions corresponding to those in a wild-type expandase selected from the group consisting of methionine 73, serine 79, valine 275, leucine 277, cysteine 281, glycine 300, asparagine 304 and isoleucine 305, provided that the amino acid substitution at the residue position of asparagine 304 is not N304L.
 2. The mutated penicillin expandase of claim 1, wherein the wild-type expandase is obtained from Streptomyces clavuligerus.
 3. The mutated penicillin expandase of claim 1, comprising an amino acid substitution at one or more residue positions selected from the group consisting of M73T, S79E, V275I, L277K, C281Y, G300V, N304K, I305L and I305M.
 4. An isolated nucleic acid molecule encoding the mutated penicillin expandase of claim
 1. 5. A recombinant vector comprising the isolated nucleic acid molecule of claim 4 and a regulatory sequence.
 6. Recombinant cells transformed with the nucleic acid molecule of claim
 4. 7. The recombinant cells of claim 6, which are penicillin G producing cells.
 8. The recombinant cells of claim 7, which are Penicillium chrysogenum cells.
 9. A method for producing a mutated penicillin expandase comprising the steps of expressing the nucleic acid molecule of claim 4 and recovering the mutated penicillin expandase.
 10. A method for producing a mutated penicillin expandase comprising the steps of culturing the recombinant cells of claim 6 to express the mutated penicillin expandase, and recovering the mutated penicillin expandase from the cell culture.
 11. A process for producing 7-aminodesacetoxycephalosporanic acid (7-ADCA) comprising the steps of treating penicillin G with the mutated penicillin expandase of claim 1 to produce phenylacetyl-7-ADCA and deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA.
 12. A process for producing 7-ADCA, which process comprises the steps of (a) cultivating penicillin G producing cells which is transformed with the nucleic acid molecule of claim 4 under the conditions suitable for production of penicillin G and expression of the mutated penicillin expandase such that the penicillin G is expanded by the mutated expandase and phenylacetyl-7-ADCA is produced; (b) deacylating the phenylacetyl-7-ADCA to produce the 7-ADCA.
 13. The process of claim 12, wherein the penicillin G producing cells are Penicillium chrysogenum cells.
 14. The process of claim 12, wherein the phenylacetyl-7-ADCA produced from Step (a) is recovered by filtration and extraction steps. 